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Estimating the key outcomes and hepatocellular carcinoma risk in patients in immune-tolerant phase of chronic hepatitis B virus infection: A systematic review and meta-analysis.
Liu, Min; Zhao, Taixue; Zhang, Jinyang; Bu, Bing; Zhang, Ruyi; Xia, Xueshan; Geng, Jiawei.
Affiliation
  • Liu M; Department of Infectious Disease and Hepatic Disease, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Zhao T; Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Zhang J; Medical School of Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Bu B; Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Zhang R; Department of Infectious Disease and Hepatic Disease, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Xia X; Department of Infectious Disease and Hepatic Disease, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.
  • Geng J; Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, Yunnan, China.
Rev Med Virol ; 34(4): e2570, 2024 Jul.
Article in En | MEDLINE | ID: mdl-38964866
ABSTRACT
The question of whether patients in the immune-tolerant (IT) phase of chronic hepatitis B virus (HBV) infection should undergo antiviral therapy and determine the optimal regimen remains unclear. A comprehensive search of PubMed, Embase, MEDLINE, Cochrane Library, and Wanfang Data from inception to 5 December 2023, was conducted. Studies reporting on key outcomes such as HBV DNA undetectability, HBeAg loss or seroconversion, HBsAg loss or seroconversion, and hepatocellular carcinoma (HCC) incidence in patients in the IT phase of chronic HBV infection were included. In total, 23 studies were incorporated. Approximately 4% of patients in the IT phase achieved spontaneous HBeAg loss over 48 weeks of follow-up. Antiviral therapy demonstrated a favourable impact on HBV DNA negative conversion (Children risk ratios [RR] = 6.83, 95% CI 2.90-16.05; Adults RR = 25.84, 95% CI 6.47-103.31) and HBsAg loss rates (Children RR = 9.49, 95% CI 1.74-51.76; Adults RR = 7.35, 95% CI 1.41-38.27) for patients in the IT phase. Subgroup analysis revealed that in adult patients in the IT phase, interferon plus nucleos(t)ide analogues (NA)-treated patients exhibited a higher pooled rate of HBsAg loss or seroconversion than those treated with NA monotherapy (9% vs. 0%). Additionally, the pooled annual HCC incidence for patients in the IT phase was 3.03 cases per 1000 person-years (95% CI 0.99-5.88). Adult patients in the IT phase had a significantly lower HCC incidence risk than HBeAg-positive indeterminate phase patients (RR = 0.46, 95% CI 0.32-0.66), with no significant differences observed between IT and immune-active phases. Presently, there is insufficient evidence solely based on reducing the risk of HCC incidence, to recommend treating patients in the IT phase of chronic HBV infection. However, both adult and paediatric patients in the IT phase responded well to antiviral therapy, showing favourable rates of HBsAg loss or seroconversion.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Carcinoma, Hepatocellular / Hepatitis B, Chronic / Hepatitis B e Antigens / Liver Neoplasms Limits: Humans Language: En Journal: Rev Med Virol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antiviral Agents / Carcinoma, Hepatocellular / Hepatitis B, Chronic / Hepatitis B e Antigens / Liver Neoplasms Limits: Humans Language: En Journal: Rev Med Virol Year: 2024 Document type: Article